Quinupristin-Dalfopristin Is Active againstToxoplasma gondii

Toxoplasmosis remains a significant problem among immunocompromised patients, infected newborns, and individuals with ocular toxoplasma involvement. Treatment of acute toxoplasmosis with pyrimethamine plus sulfadiazine or pyrimethamine plus clindamycin has been successful in most patients but may be associated with considerable toxicity (11). Thus, drugs with increased potencies and lower levels of toxicity are needed to treat all forms of toxoplasmosis.

Synercid is a new drug with a mechanism of action and antibacterial spectrum similar to those of macrolides, azalides, and ketolides (12, 13) that have been found to be active againstToxoplasma gondii (4, 9). It has activity against gram-positive and select gram-negative bacteria and comprises two semisynthetic pristinamycin derivatives, quinupristin (RP 57669; derived from pristinamycin I) and dalfopristin (RP 54476; derived from pristinamycin IIA) in a 30:70 ratio (7, 8). Because of the reported antitoxoplasma activities of the macrolides (5), azalides (1), and ketolides (4), it was considered of interest to investigate synercid and its two components for their in vitro and in vivo activities against T. gondii.

Tachyzoites of the RH strain of T. gondii were obtained from the peritoneal cavities of mice that had been infected 2 days earlier; cysts of the C56 strain were from the brains of chronically infected mice (2). Outbred female Swiss Webster mice (B & K Laboratories, Fremont, Calif.) weighing approximately 20 g at the beginning of each experiment were used. Mice were given water and food ad libitum. Synercid, quinupristin, and dalfopristin were provided by Rhône-Poulenc Rorer (Collegeville, Pa.).

For in vitro studies, human foreskin fibroblast (HFF) cells (ATCC HS68) were grown in Dulbecco’s modified Eagle’s medium (Gibco BRL, Grand Island, N.Y.) containing 100 U of penicillin, 1 μg of streptomycin per ml, and 10% heat-inactivated T. gondiiantibody-negative fetal bovine serum. In vitro activity was defined as the capacity of the drug to inhibit intracellular replication ofT. gondii and was determined by the [³H]uracil incorporation technique as described previously (10). Briefly, HFF cells were plated at 10⁴ cells/well in 96-well flat-bottom tissue culture microtiter plates, and the plates were incubated at 37°C in a 5% CO₂ incubator. After confluence, the monolayers were infected with tachyzoites at a ratio of three tachyzoites/cell. Four hours later, the monolayers were washed, the drugs were added at concentrations of from 0.0 to 25.0 μg/ml, and the cultures were incubated as described above for 48 h. Four hours prior to harvesting of the cells, [³H]uracil (1 μCi/well) was added and its level of incorporation was determined. The cells were collected with a cell harvester, and the radioactivity was counted with a scintillation counter. The toxicities of the drugs for HFF cells were determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay with the Cell Titer 96 Kit (Promega Corp., Madison, Wis.) as described previously (10).

For in vivo studies, mice were infected orally with 10 cysts of the C56 strain. Treatment was initiated 3 days later as a single daily intraperitoneal dose and was continued for 10 days. Mice were observed for mortality and time to death for 30 days from the day of infection. At the end of the 30-day period, the brains of the surviving mice were examined for the presence of cysts of T. gondii as described previously (3). P values were obtained by the log-rank test of the Kaplan-Meier product limited-survival analysis by using survival tools for StatView, version 4.02, computer software (Abacus Concepts, Berkeley, Calif.). A P value of ≤0.05 was considered statistically significant.

Synercid, quinupristin, and dalfopristin each inhibited the intracellular replication of T. gondii in vitro. Their 50% inhibitory concentrations after 48 h of exposure were 1.6, 2.7, and 6.3 μg/ml, respectively (Fig. 1A to C, respectively). Thus, synercid was more active than either of its components alone. None of the compounds showed toxicity for the host cells at concentrations that were highly active against T. gondii.

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Fig. 1.

Effects of synercid (A), quinupristin (B), and dalfopristin (C) on intracellular replication of RH tachyzoites in vitro determined by [³H]uracil incorporation and on host HFF cells in vitro determined by the MTT assay. Results are presented as means ± standard deviations for triplicate assays.

Synercid at 100 and 200 mg/kg of body weight per day administered intraperitoneally for 10 days protected 50% ( P = 0.0002) and 100% (P < 0.0001) of infected mice against death, respectively (Fig. 2A). A dosage of 50 mg/kg/day resulted only in a 2-day prolongation of the time to death that was not statistically significant. In contrast, quinupristin or dalfopristin, when administered alone, each protected only 20% (P > 0.270) of infected mice at the highest dosage tested (200 mg/kg/day) (Fig. 2B and C). Thus, synercid was fivefold more active in vivo than either of its components alone.T. gondii cysts were observed in the brains of the surviving mice in each of the groups treated with either of these drugs.

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Fig. 2.

Effect of treatment with synercid (A), quinupristin (B), or dalfopristin (C) intraperitoneally for 10 days on survival of mice infected with the C56 strain of T. gondii. There were 5 mice in the control group and 10 mice in the treatment groups.

The results presented above reveal that although synercid, quinupristin, and dalfopristin had significant in vitro activities against T. gondii, only synercid had significant in vivo activity. Synercid was more potent than either of its components alone in vitro and in vivo. Although synercid significantly protected mice against death, it did not prevent colonization of tissues by T. gondii since cysts were found in the brains of surviving mice.

The mechanism of action of synercid against T. gondii is not known. However, in bacteria, quinupristin and dalfopristin bind to the RNA of the 50S ribosomal subunit and act synergistically to inhibit protein synthesis (13). Since ribosomes encoded by prokaryotic-type ribosomal genes of T. gondii are predicted to be sensitive to the lincosamide-macrolide class of antibiotics and may serve as the functional target to protein synthesis inhibitors inT. gondii and related parasites (6), synercid may be inhibiting ribosomal protein synthesis. Our results demonstrate that the combination of quinupristin and dalfopristin has an enhanced effect against T. gondii compared to the activity of either one of them alone. It is possible that such enhancement in activity may be elicited through a mechanism similar to that observed in bacteria (13).

Pharmacokinetic studies of synercid with healthy human volunteers have revealed that the maximum concentration in blood ranges from 0.95 μg/ml after a 1-h intravenous infusion of a dose of 1.4 mg/kg to 24.2 μg/ml after infusion of a dose of 29.4 mg/kg (7). However, neither of the components of synercid significantly penetrates the central nervous systems of rats, monkeys, or humans (7). The terminal half-lives of elimination for quinupristin and dalfopristin in humans were 0.93 to 0.96 and 0.39 to 0.91 h, respectively (7). Therefore, it is evident that the concentrations of synercid that were highly active against T. gondii in vitro are achievable in the serum of humans with conventional doses. Thus, synercid may be useful for the treatment of human toxoplasmosis.

• Copyright © 1999 American Society for Microbiology